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Thioacetamide is used in qualitative inorganic analysis as an in-situ source for sulfide ions. It is used in analytical chemistry as a source of hydrogen sulfide. It is an additive in enantioselective reduction of beta-keto esters with immobilized bakers yeast. It is also used as a vulcanizing agent of polymer and a crosslinking agent.
You, M. S.; Lim, C. S.; Kwon, D. H.; Heo, J. H.; Im, S. H.; Chae, K. J. Oxide-free Sb2S3 sensitized solar cells fabricated by spin and heat-treatment of Sb (III)(thioacetamide)2Cl3. Org. Electron. 2015, 21, 155-159.
Wei, D. D.; Wang, J. S.; Li, M. H.; Guo, P. P.; Dong, G.; Yang, M. H.; Kong, L. Y. A pilot study of the onset of hepatic encephalopathy (OHE) in mice induced by thioacetamide and the protective effect of taurine by holistic metabolic characterization. Metabolomics 2015, 11 (3), 559-570.
Gefahrenhinweise (EU): H302-H315-H319-H350
Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause cancer.
Obtain special instructions before use. Wear protective gloves/protective clothing/eye protection/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.